A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027677



Internal ID19116896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28080777..28101543hg38UCSC Ensembl
Innerchr9:28080775..28101541hg19UCSC Ensembl
Innerchr9:28070775..28091541hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3820767
hg1920767
hg1820767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755879
Samples
Known GenesLINGO2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027677
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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